Reported Apr 29, 2015 · Terminated
The PCA 3 infusion pump allows clinicians, or patients, to (self) Administer analgesia safely and effectively within…
Hospira Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Hospira Inc. · 275 N Field Dr · Lake Forest, IL · 60045-2579
Is this the product you have?
- The PCA 3 infusion pump allows clinicians, or patients, to (self) Administer analgesia safely and effectively within clinician programmed limits.
- Lot codes and dates
- List 12384Serial
- Numbers
2,715 of 2,715 codes
129200411292004812920052129200561292006612920069129200791292008212920101129201021292010412920105129201061292010712920117129201211292012212920152129201581292015912920160129201741292024612920248129202511292025212920255129202571292026412920265129202681292027012920275129202761292027712920278129202821292028712920289129202911292029412920304129203051292031112920312129203201292032812920330129203321292034012920343129203461292034712920352129203531292035712920358129203591292036012920362
- Amount recalled
- 8,214 units
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was recalled
The infusion pump has a clear plastic door that, due to its design, allows for excessive flexing. This in turn permits unauthorized access to the vial of medication.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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